HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717108Generated: November 1, 2026
Boron tribromide → HCID 117992578, compound
https://huagongshe.com/reaction/717108
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 117992760 | HCID 117992760 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117992578 | HCID 117992578 | 63% |
Reaction Steps
To a stirred solution of N,N-Bis-(2-methoxy-ethyl)-4-(5-methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl)-benzamide (40 mg, 0.10 mmol) in CH2Cl2 (2.5 mL) under N2 at −78° C. was added boron tribromide (1M in CH2Cl2, 2.54 mL, 2.54 mmol). The reaction was allowed to warm to RT and stirred for 16 h. The reaction mixture was quenched with H2O and extracted with EtOAc (5 mL) upon which a pale yellow solid precipitated and was filtered off. The aqueous phase was further extracted with CH2Cl2 (5 mL). The combined organics were evaporated to dryness. Product was found to be also present in the aqueous phase and was passed through an Isolute-103 cartridge (500 mg), washing with H2O (4× column volumes). The product was eluted from the column with MeOH (4× column volumes) and evaporated to dryness. The combined crude product was purified by reverse phase preparative HPLC-MS to obtain N,N-bis-(2-hydroxy-ethyl)-4-(5-methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl)-benzamide as a white solid (23 mg, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193689B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-48aefff018bd4d53a20472c5706e828c |
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| Source note | uspto-grants-2015_11 |
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